Regional Master Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Regional Master Corp. makes
Regional Master Corp. manufactures surgical instruments and monitoring devices, including a precision gripper for tissue handling, a nerve locator for intraoperative identification, a stimulator computer for nerve testing, and a needle guidance system for targeted injections.
Their portfolio consists of Class II medical devices, each authorised through the FDA’s 510(k) clearance process. The company’s products are listed under the US regulatory framework and are based in the United States.
Catalogue
The Gripper Ref K853422
Regimes: 510(k) Registry: 510(k)Nerve Finder Ref K853477
Regimes: 510(k) Registry: 510(k)T4 Monitor Stimulator Computer Ref K853476
Regimes: 510(k) Registry: 510(k)Pinpoint Needle Ref K853478
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Regional Master Corp. have in the registry?
The registry currently lists 4 devices for Regional Master Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regional Master Corp.'s devices?
Among its 4 most recently registered devices, Regional Master Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Regional Master Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Regional Master Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Regional Master Corp. in the registry?
The most recently registered devices listed for Regional Master Corp. include THE GRIPPER, NERVE FINDER, T4 MONITOR STIMULATOR COMPUTER and PINPOINT NEEDLE.